Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1679570Generated: October 25, 2026

N-chloro-N-methyl-p-toluenesulfonamide → p-Nitrobenzyl 3-Methyl-2-(2-chlorosulfinyl-4-oxo-3-phenoxyacetamido-1-azetidinyl)-3-butenoate

https://huagongshe.com/reaction/1679570

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-chloro-N-methyl-p-toluenesulfonamideHCID 13017215—
Reactantp-Nitrobenzyl 6-phenoxyacetamido-2,2-dimethylpenam-3-carboxylate-1-oxideHCID 67928276—
Productp-Nitrobenzyl 3-Methyl-2-(2-chlorosulfinyl-4-oxo-3-phenoxyacetamido-1-azetidinyl)-3-butenoateHCID 9936995—

Reaction Steps

To 150 ml. of distilled and molecular sieve-dried toluene were added 3.0 g. (6 mmol.) of p-nitrobenzyl 6-phenoxyacetamido-2,2-dimethylpenam-3-carboxylate-1-oxide and 1.3 g. (6 mmol.) of N-chloro-N-methyl-p-toluenesulfonamide. The mixture was heated at reflux for 60 minutes. The resulting reaction mixture then was cooled to room temperature. An aliquot (15 ml.) was separated, washed with water, and brine, dried over magnesium sulfate, and evaporated to dryness in vacuo. The nmr spectrum of the residue was consistent for the title compound contaminated with some N-methyl-p-toluenesulfonamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04081440
Source datasetuspto-grants-1978_03
ORD IDord-1006accfc76e47c697b583e953dc30c6
Source noteuspto-grants-1978_03